Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017759006

FEI Number

3017759006

Entity Name

MEDICAL DEVICES GROUP LIMITED

City/State/Country

N.T., HK

Establishment Address

Unit 1, 1/F, Precision Manufacturing Centre, 3 Dai Hei Street, Tai Po Industrial Estate, N.T. --, HK

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Medical Devices Group Limited (Owner Number: 10078224)

Owner / Operator Contact Address

Unit 1, 1/F, Precision Manufacturing Centre, 3 Dai Hei Street, Tai Po Industrial Estate, N.T., HK-NOTA --, HK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JEP	Retainer, Matrix	Dental	Class 1	872.4565	2020-10-15
ECB	Unit, Syringe, Air And/Or Water	Dental	Class 1	872.4565	2020-10-15

Official Correspondent

Brian Lo

US Agent Details

Brent Geiger Email: bgeiger@medicom.com Phone: (763) 2189292

Related Public Records

Same Entity

Medical Devices Group Limited

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K831136	Almore Intl., Inc.	DOUBLE BOW TOOTH SEPARATOR	1983-06-08

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017759006. Last updated year: 2026. Please use registration number 3017759006 when referencing this establishment in official correspondence.